WITT BIOMEDICAL SERIES IV— 510(k) K950436

Substantially Equivalent

Witt Biomedical Corporation

FDA 510(k) clearance K950436 for WITT BIOMEDICAL SERIES IV, Substantially Equivalent on 1995-11-02. Applicant: Witt Biomedical Corporation.

Clearance details

Applicant: Witt Biomedical Corporation
Product code: Code MHX
Advisory panel: Cardiovascular
Date received: 1995-02-02
Decision date: 1995-11-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Melbourne, FL, US

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Adverse events under product code MHX

product code MHX

Death: 580
Injury: 2,441
Malfunction: 12,655
Other: 3
Total: 15,679

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.